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Osteogenic/Odontogenic Bioengineering with co-Administration of Simvastatin and Hydroxyapatite on Poly Caprolactone Based Nanofibrous Scaffold

机译:辛伐他汀和羟基磷灰石在聚己内酯基纳米纤维支架上的联合成骨/成牙生物工程

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摘要

>Purpose: Statin is an effective factor for promoting osteogenesis. The aim of the present study was to evaluate the effect of simvastatin (SIM) and/or HA addition on changes in osteogenesis levels by human DPSCs transferred onto three-dimensional (3D) nanofibrous Poly (ε-caprolactone) (PCL)/Poly lactic acide (PLLA) polymeric scaffolds.>Methods: For this purpose, a 3D nanofibrous composite scaffold of PCL/PLLA/HA was prepared by electrospinning method. SIM was added to scaffolds during DPSCs culturing step. Cell proliferation and osteogenic activity levels were assessed by using MTT assay and Alizarin Red assay methods. In addition, the expression of genes responsible for osteogenesis, including BMP2, Osteocalcin, DSPP and RUNX2, were determined before and 2 weeks after incorporation of SIM.>Results: The MTT assay showed that PCL/PLLA/HA scaffolds seeded with DPSCs has significant (p<0.05) more proliferative effect than PCL/PLLA or DMEM cultured cells, additionally SIM administration improved this result over the PCL/PLLA/HA scaffolds without SIM treatment. SEM imaging revealed improved adhesion and probably osteogenic differentiation of DPSCs on PCL/PLLA/HA nanofibers treated with SIM, moreover the alizarin red assay ensured significant (p<0.05) higher mineralization of this group. Finally, real time PCR confirmed the positive regulation (P<0.05) of the expression of osteo/odontogenesis markers BMP2, Osteocalcin, DSPP and RUNX2 genes in PLLA-PCL-HA (0.1)-SIM group.>Conclusion: As a result, addition of simvastatin with incorporation of hydroxyapatite in PCL-PLLA scaffolds might increase the expression of osteogenesis markers in the DPSCs, with a possible increase in cell differentiation and bone formation.
机译:>目的:他汀类药物是促进成骨的有效因子。本研究的目的是评估辛伐他汀(SIM)和/或HA的添加对人类DPSC转移到三维(3D)纳米纤维聚(ε-己内酯)(PCL)/聚乳酸中成骨水平变化的影响>方法:为此,通过静电纺丝法制备了PCL / PLLA / HA的3D纳米纤维复合支架。在DPSC的培养步骤中,将SIM添加到支架中。通过使用MTT测定法和茜素红测定法评估细胞增殖和成骨活性水平。此外,在整合SIM之前和之后2周确定了负责骨生成的基因的表达,包括BMP2,骨钙蛋白,DSPP和RUNX2。>结果: MTT分析表明PCL / PLLA / HA用DPSC接种的支架比PCL / PLLA或DMEM培养的细胞具有显着(p <0.05)的增殖作用,另外,SIM给药比未经SIM处理的PCL / PLLA / HA支架改善了这一结果。 SEM成像显示,在用SIM处理的PCL / PLLA / HA纳米纤维上,DPSCs的粘附力有所改善,并且可能是成骨细胞分化的原因,此外茜素红试验确保了该组矿物质的显着(p <0.05)更高。最后,实时荧光定量PCR证实了PLLA-PCL-HA(0.1)-SIM组骨/牙生成标记物BMP2,骨钙蛋白,DSPP和RUNX2基因表达的正调控(P <0.05)。>结论:

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